Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_assertion description "[Biallelic mutations in PALB2 cause FA (Fanconi's anaemia) subtype FA-N, a devastating inherited disorder marked by developmental abnormalities, bone marrow failure and childhood cancer susceptibility, whereas monoallelic mutations predispose to breast, ovarian and pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_assertion evidence source_evidence_literature NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_assertion SIO_000772 24870022 NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_assertion wasDerivedFrom befree-20150227 NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_assertion wasGeneratedBy ECO_0000203 NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945390.RA5lAnMe_I5cRxUZmMV6bWtfiUDy5qeP5r8USYk1tnBP0130_provenance.